腹疝人工修复术后植入区组织反应的分区研究

E. Lukoyanychev, S. Izmailov, D. Evsyukov, V. O. Nikolskij, A. A. Mironov, A. V. Panyushkin
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Microphotography was performed on a medical transmitted light microvisor Microvisor μVizo‑103 (AD LOMO, Russia) with a 3.2 Mpx matrix (full frame size 1024 × 882 px, infoband width 88 px) with Planachromat and Stigachromat lenses with a digital scale × 1 (i.e. no digital zoom). Microphoto processing was performed using the ImageJ 1.53k program (version for public use). The criterion for including a microphoto in the calculation of indicators was the presence of an ingrown implant fiber in the preparation or a cavity surrounding the implant.Results. The zone adjacent to the implant, with a width of about 50 µm (\"the zone of changes in adjacent tissues\") significantly differs from the \"zone of changes in distant tissues\" by a more pronounced inflammatory reaction due to a larger absolute number of lymphocytes (р = 0.019 and fibroblasts (р = 0.017), giant cells of foreign bodies (р < 0.001), larger vascular area (р < 0.001) and extravasations (р = 0.002). 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引用次数: 0

摘要

研究目的:应用新的数字图像处理技术,建立评估疝环修复后植入区组织反应的标准。材料和方法。实验以13只不同性别的Wistar大鼠为实验对象。在麻醉下,将一个4 × 2 cm的网状假体植入与外膜膜相似的层。每种制剂的制备和染色分为两种版本:用苏木精-伊红染色和根据马洛里在不同的眼镜上染色。进行实验的季节是冬季和夏季。显微摄影在医用透射光微遮板microvisor μVizo‑103 (AD LOMO, Russia)上进行,采用3.2 Mpx矩阵(全帧尺寸1024 × 882 px,信息带宽度88 px),采用数字比例× 1的Planachromat和Stigachromat镜头(即无数字变焦)。显微照片处理使用ImageJ 1.53k程序(公众使用版本)。在计算指标时包括显微照片的标准是在制备过程中是否存在向内生长的植入物纤维或植入物周围是否存在腔体。与植入物相邻的区域,宽度约为50µm(“相邻组织改变区”)与“远处组织改变区”明显不同,由于淋巴细胞的绝对数量更多(0.019和成纤维细胞(0.017),异物巨细胞(< 0.001),更大的血管面积(< 0.001)和外渗(< 0.002),炎症反应更明显。“邻近组织变化区”的研究对于评估机体对植入的局部反应至关重要。确定种植区域的关键区域:“种植体周围的空腔”、“邻近组织的变化区”、“远处组织的变化区”。这些区域内指标的计算可以让你在实验中比较研究小组时得到更详细的结果。本文提出了一种利用新型数字成像技术评估人工疝修补术后植入区组织反应的有效方法,该方法可在常规光学显微镜和标准染色方法下使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Zoning of the reaction of the tissues of the implantation area after prosthetic repair in abdominal hernias in experiment
Purpose of the study. Development of criteria for evaluating the reaction of tissues in the implantation area after prosthetic repair of the hernia ring in an experiment using new digital image processing technologies.Materials and methods. The experiment was carried out on 13 Wistar rats of different sexes. Under anesthesia, a 4 × 2 cm mesh prosthesis was implanted in the layer similar to the onlay epiaponeurotic. The preparation and staining of each preparation was carried out in two versions: with hematoxylin-eosin and according to Mallory on different glasses. The seasons for performing experiments are winter, summer. Microphotography was performed on a medical transmitted light microvisor Microvisor μVizo‑103 (AD LOMO, Russia) with a 3.2 Mpx matrix (full frame size 1024 × 882 px, infoband width 88 px) with Planachromat and Stigachromat lenses with a digital scale × 1 (i.e. no digital zoom). Microphoto processing was performed using the ImageJ 1.53k program (version for public use). The criterion for including a microphoto in the calculation of indicators was the presence of an ingrown implant fiber in the preparation or a cavity surrounding the implant.Results. The zone adjacent to the implant, with a width of about 50 µm ("the zone of changes in adjacent tissues") significantly differs from the "zone of changes in distant tissues" by a more pronounced inflammatory reaction due to a larger absolute number of lymphocytes (р = 0.019 and fibroblasts (р = 0.017), giant cells of foreign bodies (р < 0.001), larger vascular area (р < 0.001) and extravasations (р = 0.002). The study of the "zone of changes in adjacent tissues" is of key importance in assessing the local response of the body to implantation. The key zones of the implantation area are identified: "the cavity surrounding the implant", "the zone of changes in adjacent tissues", "the zone of changes in distant tissues". The calculation of indicators within these zones allows you to get more detailed results when comparing study groups in the experiment.Conclusion. An effective method for assessing the reaction of tissues in the implantation area after prosthetic hernia repair in an experiment using new digital imaging technologies that can be used using a conventional optical microscope and standard staining methods is proposed.
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